Webinars and Sponsored Roundtables — Register Now

Wednesday, July 15, 2026, 1:00-2:00 PM ET
Hear an expert discuss how to integrate Kappa and Lambda in situ hybridization testing into your standard hematopathology workflow to accurately assess B-cell and plasma cell clonality. You will also gain the skills to recognize testing pitfalls in challenging reactive versus neoplastic proliferations and apply ancillary tools to resolve complex cases.

Webinar presenter Xiaojun Wu, MD, PhD, Assistant professor, Director of Hematopathology Section at NCR of Johns Hopkins Medicine Department of Pathology, SOM at Johns Hopkins University

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Tuesday, July 21, 2026, 11:00-11:30 AM CT

Learning Objectives:
  • Explain how transparency and manufacturer partnerships improve quality, consistency, and decision-making confidence in specimen management.
  • Evaluate blood collection tubes beyond cost and commodity assumptions, incorporating clinical impact and risk into decision-making.
  • Assess the potential risk points when using a blood collection device that has not been cleared for a specific purpose.

Roundtable presenters Nick Fingland, PhD, PMP, Senior Director, R&D Operations and Science, BD, and Chris Farnsworth, PhD, D(ABCC), Section Head of Clinical Chemistry, Professor of Pathology and Immunology, Washington University School of Medicine.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Wednesday, July 29, 2026, 1:00-2:00 PM ET
Learn about digital pathology technology that is future-ready, yet practical for today’s
laboratory needs.

Webinar presenters Scott Hammond, Senior Systems Consultant, Digital Pathology Division, Wexner Medical Center, Department of Pathology, and Ursula Hofer, Imaging Technologist, Pathology Digital Imaging Lab, Wexner Medical Center, Department of Pathology, and Sandra Banky, PA(ASCP), Director of Operations, Wexner Medical Center, Department of Pathology.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Next-Generation Sequencing, 2024

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Next-gen sequencing—the anxiety, optimism, and goal

Laboratory-developed testing as it relates to next-generation sequencing was up first in the NGS conversation led online by CAP TODAY publisher Bob McGonnagle on March 19. Other topics: in-house NGS testing, artificial intelligence, and bioinformatics. “There’s a reality now where bioinformatics is solid, stable, and reliable,” said José Luis Costa, PhD, of Thermo Fisher Scientific.

May 2024—Laboratory-developed tests are top of mind for many people in laboratories. People who use next-generation sequencing panels and machines are, in many cases, heavily involved in laboratory-developed tests, in addition to the panels that many companies offer. Larissa Furtado, talk to us about the role of laboratory-developed tests in the context of next-generation sequencing testing.

Larissa V. Furtado, MD, molecular pathologist, St. Jude Children’s Research Hospital: They’re essential. In our practice, all the oncology NGS tests we have in-house are laboratory-developed tests. We don’t have FDA-approved tests.

Next-generation sequencing is a technology that evolves quickly. You can test multiple genomic anomalies at different genes simultaneously and multiple samples at one time. The flexibility of LDTs gives laboratories the ability to develop their own tests and update them according to their needs. I am in a pediatric hospital where most of our patients are in clinical trials, so we have a comprehensive testing approach, which may be different from other centers or smaller laboratories that use more targeted testing. With the existing accreditation requirements and framework, pathologists are well positioned to bring in these tests and ensure quality.

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